Figure 1.
GAS6/AXL expression is highly increased in primitive AML patient cells. (A) qRT-PCR results for AXL and GAS6 transcript levels in unpurified (FH/NH4CL) cells, CD34+ stem/progenitor cells, and CD34− cells from patients with AML (CD34+ cells from 18 samples and CD34− from 6 samples). (B) qRT-PCR results for AXL and GAS6 transcript levels in stem cell–enriched CD34+CD38−, CD34+CD38+ progenitor and CD34− mature cells from patients with AML. (C) Dot plot of AXL vs GAS6 transcript levels in MLL (n = 10) and non-MLL (n = 6) primary AML samples. (D) RNA-seq analysis of transcript levels of AXL and GAS6 in MLL (n = 9) and non-MLL (n = 296) samples from patients with AML obtained from the Beat AML program. (E-F) FACS graphs of AXL-APC+ surface staining in CD34+ AML and NBM cells from cohort 1 (left panel: AML, n = 10 and NBM, n = 3) and representative samples from cohort 2 (right panel: AML, n = 12 and NBM, n = 6) (E) with corresponding quantification of mean fluorescence intensity in all samples from both cohorts (F). (G-H) FACS graphs of AXL-APC+ staining in CD34+CD38− AML and NBM cells from cohort 1 (AML, n = 10 and NBM, n = 3) (G), with corresponding quantification of mean fluorescence intensity (H). The P values were calculated using a 2-tailed, unpaired Student t test or 1-way ANOVA with Tukey’s post hoc correction for multiple comparisons.

GAS6/AXL expression is highly increased in primitive AML patient cells. (A) qRT-PCR results for AXL and GAS6 transcript levels in unpurified (FH/NH4CL) cells, CD34+ stem/progenitor cells, and CD34 cells from patients with AML (CD34+ cells from 18 samples and CD34 from 6 samples). (B) qRT-PCR results for AXL and GAS6 transcript levels in stem cell–enriched CD34+CD38, CD34+CD38+ progenitor and CD34 mature cells from patients with AML. (C) Dot plot of AXL vs GAS6 transcript levels in MLL (n = 10) and non-MLL (n = 6) primary AML samples. (D) RNA-seq analysis of transcript levels of AXL and GAS6 in MLL (n = 9) and non-MLL (n = 296) samples from patients with AML obtained from the Beat AML program. (E-F) FACS graphs of AXL-APC+ surface staining in CD34+ AML and NBM cells from cohort 1 (left panel: AML, n = 10 and NBM, n = 3) and representative samples from cohort 2 (right panel: AML, n = 12 and NBM, n = 6) (E) with corresponding quantification of mean fluorescence intensity in all samples from both cohorts (F). (G-H) FACS graphs of AXL-APC+ staining in CD34+CD38 AML and NBM cells from cohort 1 (AML, n = 10 and NBM, n = 3) (G), with corresponding quantification of mean fluorescence intensity (H). The P values were calculated using a 2-tailed, unpaired Student t test or 1-way ANOVA with Tukey’s post hoc correction for multiple comparisons.

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